| Literature DB >> 10980742 |
O A Bodamer1, D Halliday, J V Leonard.
Abstract
Myopathy in glycogen storage disease type II (GSD-II) is slowly progressive. Five subjects with the late-onset form of GSD-II (age range, 15 to 47 years) and seven healthy control subjects (age range, 28 to 55 years) were studied. Following alanine supplementation, resting energy expenditure decreased in patients with GSD-II (p < 0.05) compared to values seen in control subjects. Leucine flux decreased (p < 0.004), as did leucine oxidation, to levels lower than those observed in control subjects (p < 0.001). l-Alanine reduces protein turnover and catabolism in GSD-II.Entities:
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Year: 2000 PMID: 10980742 DOI: 10.1212/wnl.55.5.710
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910